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Changes in Appetitive Associative Strength Modulates Nucleus Accumbens, But Not Orbitofrontal Cortex Neuronal Ensemble Excitability.食欲性联想强度的变化调节伏隔核,但不调节眶额皮质神经元集群兴奋性。
J Neurosci. 2017 Mar 22;37(12):3160-3170. doi: 10.1523/JNEUROSCI.3766-16.2017. Epub 2017 Feb 17.
2
Role of Dorsomedial Striatum Neuronal Ensembles in Incubation of Methamphetamine Craving after Voluntary Abstinence.背内侧纹状体神经元集群在自愿戒断后甲基苯丙胺渴求的酝酿过程中的作用。
J Neurosci. 2017 Jan 25;37(4):1014-1027. doi: 10.1523/JNEUROSCI.3091-16.2016.
3
Distinct memory engrams in the infralimbic cortex of rats control opposing environmental actions on a learned behavior.大鼠眶下皮质中不同的记忆印迹控制着对习得行为的相反环境作用。
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Distinct Fos-Expressing Neuronal Ensembles in the Ventromedial Prefrontal Cortex Mediate Food Reward and Extinction Memories.腹内侧前额叶皮层中不同的Fos表达神经元群介导食物奖赏和消退记忆。
J Neurosci. 2016 Jun 22;36(25):6691-703. doi: 10.1523/JNEUROSCI.0140-16.2016.
5
Associative Learning Drives the Formation of Silent Synapses in Neuronal Ensembles of the Nucleus Accumbens.联合学习驱动伏隔核神经元集群中沉默突触的形成。
Biol Psychiatry. 2016 Aug 1;80(3):246-56. doi: 10.1016/j.biopsych.2015.08.006. Epub 2015 Aug 14.
6
Experience-induced Arc/Arg3.1 primes CA1 pyramidal neurons for metabotropic glutamate receptor-dependent long-term synaptic depression.经验诱导的 Arc/Arg3.1 使 CA1 锥体神经元对代谢型谷氨酸受体依赖性长时程突触抑制敏感。
Neuron. 2013 Oct 2;80(1):72-9. doi: 10.1016/j.neuron.2013.07.020.
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Drug-primed reinstatement of cocaine seeking in mice: increased excitability of medium-sized spiny neurons in the nucleus accumbens.药物激发的可卡因觅药行为复燃:伏隔核中中型棘神经元兴奋性增加。
ASN Neuro. 2013 Oct 2;5(4):257-71. doi: 10.1042/AN20130015.
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Bidirectional modulation of cocaine expectancy by phasic glutamate fluctuations in the nucleus accumbens.伏隔核中相位性谷氨酸波动对可卡因预期的双向调制。
J Neurosci. 2013 May 22;33(21):9050-5. doi: 10.1523/JNEUROSCI.0503-13.2013.
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Serotonin spillover onto the axon initial segment of motoneurons induces central fatigue by inhibiting action potential initiation.血清素溢出到运动神经元的轴突起始段,通过抑制动作电位起始引起中枢疲劳。
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From the ventral to the dorsal striatum: devolving views of their roles in drug addiction.从腹侧纹状体到背侧纹状体:对它们在药物成瘾中作用的不断发展的观点。
Neurosci Biobehav Rev. 2013 Nov;37(9 Pt A):1946-54. doi: 10.1016/j.neubiorev.2013.02.010. Epub 2013 Feb 21.

可卡因给药和 Fos-GFP 小鼠的消退记忆检索后纹状体神经元集合兴奋性的区域差异。

Regional Differences in Striatal Neuronal Ensemble Excitability Following Cocaine and Extinction Memory Retrieval in Fos-GFP Mice.

机构信息

Sussex Neuroscience, Sussex Addiction Research and Intervention Centre (SARIC), School of Psychology, University of Sussex, Falmer, UK.

出版信息

Neuropsychopharmacology. 2018 Mar;43(4):718-727. doi: 10.1038/npp.2017.101. Epub 2017 May 25.

DOI:10.1038/npp.2017.101
PMID:28540927
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5809776/
Abstract

Learned associations between drugs of abuse and the drug administration environment have an important role in addiction. In rodents, exposure to a drug-associated environment elicits conditioned psychomotor activation, which may be weakened following extinction (EXT) learning. Although widespread drug-induced changes in neuronal excitability have been observed, little is known about specific changes within neuronal ensembles activated during the recall of drug-environment associations. Using a cocaine-conditioned locomotion (CL) procedure, the present study assessed the excitability of neuronal ensembles in the nucleus accumbens core and shell (NAc and NAc), and dorsal striatum (DS) following cocaine conditioning and EXT in Fos-GFP mice that express green fluorescent protein (GFP) in activated neurons (GFP+). During conditioning, mice received repeated cocaine injections (20 mg/kg) paired with a locomotor activity chamber (Paired) or home cage (Unpaired). Seven to 13 days later, both groups were re-exposed to the activity chamber under drug-free conditions and Paired, but not Unpaired, mice exhibited CL. In a separate group of mice, CL was extinguished by repeatedly exposing mice to the activity chamber under drug-free conditions. Following the expression and EXT of CL, GFP+ neurons in the NAc (but not NAc and DS) displayed greater firing capacity compared to surrounding GFP- neurons. This difference in excitability was due to a generalized decrease in GFP- excitability following CL and a selective increase in GFP+ excitability following its EXT. These results suggest a role for both widespread and ensemble-specific changes in neuronal excitability following recall of drug-environment associations.

摘要

滥用药物与给药环境之间的习得性关联在成瘾中起着重要作用。在啮齿动物中,暴露于与药物相关的环境会引起条件性运动激活,这种激活在消退(EXT)学习后可能会减弱。尽管观察到广泛的药物诱导的神经元兴奋性变化,但对于在回忆药物-环境关联时激活的神经元集合中的特定变化知之甚少。本研究使用可卡因条件性运动(CL)程序,在表达激活神经元中绿色荧光蛋白(GFP)的 Fos-GFP 小鼠中评估了伏隔核核心和壳(NAc 和 NAc)以及背侧纹状体(DS)中的神经元集合的兴奋性可卡因条件和 EXT 后。在条件作用期间,小鼠接受重复的可卡因注射(20mg/kg),并与运动活动室(配对)或家庭笼(未配对)配对。7 到 13 天后,两组均在无药物条件下重新暴露于活动室内,并且仅配对而不是未配对的小鼠表现出 CL。在另一组小鼠中,通过反复将小鼠暴露于无药物条件下的活动室内,使 CL 消退。在 CL 的表达和 EXT 之后,与周围的 GFP-神经元相比,NAc(但不是 NAc 和 DS)中的 GFP+神经元显示出更大的放电能力。这种兴奋性差异是由于 CL 后 GFP-兴奋性的普遍降低和 EXT 后 GFP+兴奋性的选择性增加所致。这些结果表明,在回忆药物-环境关联后,神经元兴奋性的广泛变化和集合特异性变化都起着作用。